Properties of R plasmid R772 and the corresponding pilus-specific phage PR772.

R plasmid R772 was isolated from a strain of Proteus mirabilis and is a self-transmissible P-1 incompatibility group plasmid having a molecular weight of about 27 x 10(6). It renders bacterial hosts resistant to kanamycin. Phage PR772 was isolated as a phage dependent on the presence of R772 in bacterial hosts. It is hexagonal-shaped with a diameter of 53 nm, has a thick inner membrane and no tail. Vaguely defined appendages are sometimes apparent at some vertices and the phage possesses double-stranded DNA. The DNA has a guanine plus cytosine molar content of 48%. The phage is sensitive to chloroform and has a buoyant density of 1.26 g cm(-3). These observations suggested that the inner membrane of the phage could contain lipid. Phage PR772 differs in morphology from the double-stranded DNA plasmid-specific phages PR4 and PRR1 which adsorb to tips and sides, respectively, of sex pili coded for by P-1 incompatibility group plasmids. Phage PR772 formed clear plaques which varied in diameter. Serologically, phages PR772 and PR4 are possibly related though very distantly, but the two phages have identical host ranges. Phage PR772 adsorbed by one of its apices to tips of sex pili coded for by plasmid R772 in Escherichia coli. It also formed plaques on Salmonella typhimurium Proteus morganii and Providence strains harbouring this plasmid as well as strains of E. coli carrying plasmids of incompatibility groups N or W. The phage produced areas of partial clearing on lawns of P. mirabilis PM5006 harbouring plasmid R772, the P-1 incompatibility group plasmid RP4, the W group plasmid RSa or the N group plasmid N3, and on lawns of Providence strain P29 carrying plasmid RP4.

[1]  W. Hayes,et al.  Experiments in microbial genetics , 1968 .

[2]  S. Baumberg,et al.  Unusual characteristics of the receptor for the N sex factor-specific filamentous phage IKe. , 1975, Genetical research.

[3]  N. Datta,et al.  Host ranges of R factors. , 1972, Journal of general microbiology.

[4]  D. E. Bradley The occurrence of pili associated with a plasmid of the W compatibility group. , 1975, Biochemical and biophysical research communications.

[5]  J. N. Coetzee Mobilization of the Proteus mirabilis chromosome by R plasmid R772. , 1978, Journal of general microbiology.

[6]  E. S. Anderson,et al.  Molecular Studies of R Factor Compatibility Groups , 1973, Journal of bacteriology.

[7]  J. Vinograd,et al.  The evaluation of standard sedimentation coefficients of sodium RNA and sodium DNA from sedimentation velocity data in concentrated NaCl and CsCl solutions. , 1965, Biochimica et biophysica acta.

[8]  J. N. Coetzee High frequency transduction of kanamycin resistance in Proteus mirabilis. , 1974, Journal of general microbiology.

[9]  J. A. Smit,et al.  Properties of Proteus mirabilis phage 13vir. , 1970, The Journal of general virology.

[10]  D. E. Bradley Evidence for the retraction of Pseudomonas aeruginosa RNA phage pili. , 1972, Biochemical and biophysical research communications.

[11]  L. Bryan,et al.  Further properties of P-2 R-factors of Pseudomonas aeruginosa and their relationship to other plasmid groups. , 1975, Canadian journal of microbiology.

[12]  V. Iyer,et al.  A new filamentous bacteriophage with sex-factor specificity. , 1972, Virology.

[13]  D. E. Bradley Adsorption of the R-specific bacteriophage PR4 to pili determined by a drug resistance plasmid of the W compatibility group. , 1976, Journal of general microbiology.

[14]  S. Falkow,et al.  Polynucleotide sequence relationships among plasmids of the I compatibility complex. , 1974, Journal of general microbiology.

[15]  P. Doty,et al.  Determination of the base composition of deoxyribonucleic acid from its thermal denaturation temperature. , 1962, Journal of molecular biology.

[16]  S. Baumberg,et al.  Variation in expression of sex factor genes in the Proteus-Providencia group relative to Escherichia coli , 1975, Journal of bacteriology.

[17]  O. Prozesky,et al.  Properties of Providence and Proteus morganii transducing phages. , 1966, Journal of general microbiology.

[18]  J. Marmur,et al.  [109] Use of ultraviolet absorbance-temperature profile for determining the guanine plus cytosine content of DNA , 1968 .

[19]  D. E. Bradley,et al.  Adsorption of Lipid-containing Bacteriophages PR4 and PRD1 to Pili Determined by a P-1 Incompatibility Group Plasmid , 1977 .

[20]  R. Franklin Structure and synthesis of bacteriophage PM2, with particular emphasis on the viral lipid bilayer. , 1974, Current topics in microbiology and immunology.

[21]  N. Datta,et al.  fi− R Factors giving Chloramphenicol Resistance , 1971, Nature.

[22]  J. Williams,et al.  Cotransduction of morganocinogenic plasmid 174 and R factor R772. , 1977, Journal of general microbiology.

[23]  F. Leggett,et al.  Absence of a pilus receptor for filamentous phage IKe , 1974, Nature.

[24]  D. E. Bradley,et al.  Shortening of Pseudomonas aeruginosa pili after RNA-phage adsorption. , 1972, Journal of general microbiology.